| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.24143512G>A | CA122511 | THRB | c.727C>T (p.Arg243Trp) c.*1356C>T (n.*1356C>T) c.772C>T (p.Arg258Trp) c.634C>T (p.Arg212Trp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.24143512G>C | CA351891327 | THRB | c.727C>G (p.Arg243Gly) c.*1356C>G (n.*1356C>G) c.772C>G (p.Arg258Gly) c.634C>G (p.Arg212Gly) | ClinVar dbSNP |